THE COURSE OF ISCHEMIC HEART DISEASE IN A PATIENT WITH HEREDIC THROMBOPHILIA BASED ON A MUTATION IN THE PAI-1 GENE (CLINICAL CASE)

Authors

  • H. V. Svitlyk Danylo Halytsky Lviv National Medical University
  • V. M. Salo Danylo Halytsky Lviv National Medical University
  • M. O. Harbar Danylo Halytsky Lviv National Medical University
  • M. V. Myhovych Danylo Halytsky Lviv National Medical University
  • R. A. Kovalchuk Danylo Halytsky Lviv National Medical University
  • Yu. O. Svitlyk Danylo Halytsky Lviv National Medical University

DOI:

https://doi.org/10.11603/1811-2471.2021.v.i2.12227

Keywords:

coronary artery disease, plasminogen activator inhibitor 1, gene mutations, thrombosis, acute coronary syndrome

Abstract

Genetically determined hemostasis defects can often increase the risk of thrombotic events.

The aim – to find out the features of coronary artery disease (CHD) in a patient with a mutation in the PAI-1 gene.

Material and Methods. The course of coronary artery disease was analyzed taking into account the history, the results of laboratory tests, ECG data, echocardiography, coronary angiography.

Results. The course of coronary artery disease was characterized by frequent hospitalizations for acute coronary syndrome and steady progression of atherosclerotic changes in the coronary arteries. Dual antithrombotic therapy (rivaroxaban, 15 mg; clopidogrel, 75 mg daily) and high-intensity statin therapy reduced coronary events.

Conclusions. Diagnosing of hereditary thrombophilia and optimization of treatment strategy can improve the course of coronary artery disease.

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Published

2021-07-28

How to Cite

Svitlyk, H. V., Salo, V. M., Harbar, M. O., Myhovych, M. V., Kovalchuk, R. A., & Svitlyk, Y. O. (2021). THE COURSE OF ISCHEMIC HEART DISEASE IN A PATIENT WITH HEREDIC THROMBOPHILIA BASED ON A MUTATION IN THE PAI-1 GENE (CLINICAL CASE). Achievements of Clinical and Experimental Medicine, (2), 206–212. https://doi.org/10.11603/1811-2471.2021.v.i2.12227

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